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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2096957생성일: 2026년 10월 26일

N,N,N',N'-Tetramethylethylenediamine → 6'-Bromospiro[cyclopentane-1,3'-indolin]-2'-one

https://huagongshe.com/reaction/2096957

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물1,4-DiiodobutaneHCID 12337—
반응물Ammonium ChlorideHCID 25517—
반응물6-bromo-2,3-dihydro-1H-indol-2-oneHCID 2773289—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물6'-Bromospiro[cyclopentane-1,3'-indolin]-2'-oneHCID 1271709045.6%

반응 조건

온도-20 °C

반응 단계

n-Butyl lithium (2.5 M in hexanes, 3.8 mL, 9.5 mmol) was added dropwise over 30 minutes to a stirred suspension of 6-bromoindolin-2-one (preparation 1, 1.00 g, 4.7 mmol) and N,N,N′,N′-tetramethylethylenediamine (1.42 mL, 9.4 mmol) in tetrahydrofuran (20 mL) at −78° C. The mixture was stirred for 1 hour, then 1,4-diiodobutane (3.11 mL, 23.6 mmol) was added dropwise over 5 minutes. The mixture was warmed to −20° C. over a 1 hour period, was stirred for a further hour at this temperature and was then warmed to room temperature. After 3 hours stirring at room temperature, saturated aqueous ammonium chloride solution was added to the reaction and the mixture was extracted with ethyl acetate. The organic layer was washed with water, brine, dried (MgSO4) and evaporated. Purification of the residue by flash chromatography (10:1 hexanes/ethyl acetate) gave the title compound (0.57 g, 45%) as a pale pink solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08450341B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-4e9641845ee34b83a1e636ba7d59c737
출처 메모uspto-grants-2013_05